ICON Clinical Research Associate job vacancy
Clinical Research Associate
About the role
As a (job title) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
What you will be doing:
Performing monitoring visits according to plan, document actions and follow up on action plans
Site feasibility visits incl. analysis of site logistics, site personnel performance/quality indicators and accountability for patient recruitment strategies
Train and guide site staff in the protocol and trial procedures to minimize protocol deviations (PDs)
Train site staff in safety information handling and systems
Know and meet all local and company requirements with respect to safety reporting
Proactive use of EDC and other data source systems for preparation and conduct of site visits as well as source data verification in collaboration with data management/logistics team
Identify potential risks and proactively take action to prevent or mitigate
Collaborate with Data Management/logistics in resolving queries
Ensure data cleaning cycle timelines are met in accordance with the Data Flow Plan
Manage trial product requirements, incl. temperature deviations and training of site staff
Motivate and build strong relations with site personnel to ensure NN is their preferred clinical research partner
Ensure collaboration with and deliverables from vendors locally, if applicable
Collection and management of essential documents
Primary point of contact between site staff and NN. Acts as ambassador for the company and contributes to making NN the preferred partner.
Responsible for taking leadership of site management for the selection and initiation of sites as well as conduct and closing activities of the appointed studies in compliance with local regulations, ICH-GCP,
NN procedures and protocol requirements to ensure data quality and study subject protection.
Responsible for managing the site to meet patient recruitment rate and target.
Delivers results that have direct impact on the successful completion of the clinical program.
Coordinates with PM and communicates to them progress and critical issues that may impair trial progress.